Certain geranyl phenyl ethers

ABSTRACT

Compounds having the formula   IN WHICH R is hydrogen, lower alkyl, lower alkenyl, lower alkoxy, halogen, nitro; or lower alkylthio; X is chlorine or bromine; A and B are each hydrogen, together form an epoxide link or together form a bond; the use of these compounds in controlling insects; and a method of preparing these compounds.

United States Patent [191 Pallos et a1.

[ Oct. 21, 1975 Related US. Application Data [62] Division of Ser. No. 376,787, July 5, 1973, which is a division of Ser. No. 198,018, Nov. 4, 1971, Pat. No. 3,772,365.

[52] US. Cl...... 260/612 D; 260/609 F; 260/613 D; 424/340; 424/341; 424/337; 424/278 [51] Int. Cl. C07C 43/20 [58] Field of Search 260/612 D, 613 D [56] References Cited UNITED STATES PATENTS 3,267,169 8/1966 Smutny 260/612 D X 3,787,443 1/1974 Erickson.... 260/612 D X 3,828,031 8/1974 Karrer 260/612 D X OTHER PUBLICATIONS Sarmiento et al., Science, Vol. 179, (1973), pp. 1342-1343.

Slama et al., Proceeding of the National Academy of Sciences, Vol. 54, (1965), pp. 411-414.

Primary Examiner-Bernard Helfin Attorney, Agent, or Firm-Edwin H. Baker [5 7] ABSTRACT Compounds having the formula in which R is hydrogen, lower alkyl, lower alkenyl, lower alkoxy, halogen, nitro; or lower alkylthio; X is chlorine or bromine; A and B are each hydrogen, together form an epoxide link or together form a bond; the use of these compounds in controlling insects; and a method of preparing these compounds.

4 Claims, No Drawings CERTAHN GERANYL PHENYL ETHERS This is a division, of application Ser. No. 376,787, filed July 5, 1973, which is a division of application Ser. No. 198,018, filed Nov. 4, 1971, now U.S. Pat. No. 3,772,365.

This invention relates to the use of certain novel chemical compounds in controlling insects, more particularly, the chemical compounds are certain derivatives of phenyl geranyl ethers. The invention also relates to a method of preparing the compounds.

It has been found that there is a class of compounds which acts in a different manner on insects than presently used insecticides and exerts a disrupting influence upon the normal development of insects. Such compounds impede the metamorphosis of the normal pupation of pest insects and result in the formation of numbers of the treated species which are not-viable or sterile. This ultimately leads, indirectly at least, to the destruction of a pest population.

The compounds of the present invention are believed to have further advantages that they are non-toxic to warm-blooded animals and highly effective to control insects at low dosages. It is also hoped that it will 'be more difficult for insects to develop resistance against these compounds.

One embodiment of the present invention is concerned with novel pesticidal compositions.

In another embodiment, the invention is concerned with the active pesticidal component of such compositions.

In still another embodiment, the invention is con cerned with a process for controlling insects by hinderin which R is hydrogen; halogen; lower alkyl having 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms; lower alkoxy having 1 to 4 carbon atoms, preferably 1 to 2 carbon atoms; lower alkenyl, having 2 to 6 carbon atoms, preferably 3 to 4 carbon atoms; lower alkylthio having 1 to 4 carbon atoms, preferably 1 to 2 carbon atoms, or nitro, most preferably, R is in the paraposition; X is chlorine or bromine; and A and B are each hydrogen, together form an epoxide link or to gether form a bond. The term halogen covers chlorine, bromine, iodine and fluorine.

Carbon atoms, joined to two or less hydrogen atoms, occupy each angle in the backbone of the compound represented by the above formula unless otherwise specified. Letters at the terminals and branches have been used to show the attached groups.

The certain halogenating agents recited herein are t-alkyl hypochlorite, preferably t-butyl hypochlorite;

t-alkyl hypobromite, preferably t-butyl hypobromite; HOCl, HOBr; or N-bromoimides, preferably N- bromosuccinimide.

As indicated heretofore, the above compounds are useful in impeding the metamorphosis and/or the reproduction of insects. The activity of the compounds is such that insects at any stage of their development can be effectively treated therewith.

Reaction No. l

The compound having the formula in which R and X are defined can be prepared by the following reaction:

+ Certain Halogenating Agent Reaction No. 2

The compounds having the formula in which R and X are as defined, can be prepared by the following reaction:

+ epoxidiz ing agent in which R and X are as defined.

Preferably, reaction number 2 is carried out in a solvent such as methylene chloride, preferably the epoxidizing agent is added slowly with stirring at a tempera- Reaction No. 3

Compounds having the formula in which R and X are as defined, can be prepared by the following reactions:

-l- Certain Halogenating Agent in which R is as defined.

Preferably, reaction number 3 is carried out in a solvent such as methylene, chloride, preferably the certain halogenating agent is added slowly with stirring and at a temperature sufficient to give a controlled reaction, such as about C. to about C. Preferably reaction number 3 is carried out using about equal mole amounts of the reactants, or with a slight excess of the halogenating agent. The reaction product is recovered by conventional means.

A process of this invention is one for preparing a compound of the formula:

in which R is hydrogen; halogen, lower alkyl having 1 to 6 carbon atoms; lower alkoxy having 1 to 4 carbon atoms; lower alkenyl having 2 to 6 carbon atoms; lower alkylthio having 1 to 4 carbon atoms; or nitro; and C and D are each hydrogen, or together form a bond comprising the step of reacting a compound of the formula:

in which R, C and D are as defined with t-butyl hypochlorite, or HOCl.

Preferably, the reaction is carried out in a solvj-nt such as methylene chloride, preferably the recites chlorinating agent is added slowly with stirring and at a temperature sufficient to give a controlled reaction, such as about 0C. to about 10C. Preferably the reaction is carried out using about equal mole amounts of the reactants, or with a slight excess of the chlorinating agent. The reaction product is recovered by conventional means. Another process of this invention is one for preparing a compound of the formula:

in which R is hydrogen; halogen; lower alkyl having I to 6 carbon atoms; lower alkoxy having l to 4 carbon atoms; lower alkenyl having 2 to 6 carbon atoms; lower alkylthio having 1 to 4 carbon atoms; or nitro; and C and D are each hydrogen, or together form a bond comprising the step of reacting a compound of the formula:

in which R, C and D are as defined with t-butyl hypobromite HOBr or N-bromosuccinimide.

Preferably the reaction is carried out in a solvent such as methylene chlorine, preferably the brominating agent is added slowly with stirring and at a temperature sufficient to give a reaction is carried out using about equal mole amounts of the reactants, or with a slight excess of the brominating agent. The reaction product is recovered by conventional means. Preparation of the compounds of this invention is illustrated by the following specific examples.

Br D EXAMPLE I l-(4-ethyl) phenoxy-3,7-dimethyl-6-chloro-2,7-octadiene 2.58 g. (0.0l mole) of a compound of the formula is dissolved in 25 ml. CH Cl and cooled in an ice bath. Slowly 1.1 g. (0.01 mole) t-butylhypochlorite in 10 ml. CH Cl is added dropwise at a temperature of 5C. The mixture is stirred in an ice bath for /2 hour and at room temperature for 1 hour and allowed to stand overnight. The reaction product is worked up by adding 15 ml. CH Cl and the mixture is washed with water, with NaHCO twice, dried over MgSO filtered and stripped to yield 2.3 g. of the desired product, N P 1.5200. The structure is confirmed by I.R., n.m.r. and mass spectroscopy.

EXAMPLE ll 1-(4-ethyl) phenoxy-3,7-dimethyl-6-chloro-2,7-octadiene 12.5 ml. of a 5.5% solution of NaOCl are stirred and cooled in an ice bath. A mixture of 2.58 gr. (0.01 mole) of a compound of the formula and 0.7 gr. CH COOH acetic acid glacial are added at once. The acetic acid and the NaOCl react to form HCCl in situ. Temperature goes from 8C. to 26C. The mixture is stirred for hour. The reaction product is recovered by adding CH CI separating the organic layer. This is washed with 10% NaHCO solution, dried over MgSO filtered and stripped to yield 2.1 gr. of the desired product N 1.5220. The structure is confirmed by l. R. and n.m.r. spectroscopy.

EXAMPLE lll l-(4'-ethyl) phenoxy-3,7-dimethyl-6-bromo-2,7-octadiene 1.3 gr. (0.005 mole) of a compound of the formula is dissolved in 15 ml. 1,2-dimethoxyethane and 1.8 gr. (0.015 mole) N-bromosuccinimide are mixed at a temperature of 0C. to 5C. and stirred at room temperature overnight. The mixture is evaporated to dryness with a water aspirator. ml. CCL, is added and the mixture stirred. A solid form is removed by filtration. The solid is washed with CCl The organic layers are combined, washed twice with water, dried over MgSO filtered and stripped. 1.9 gr. of the desired product is obtained, N 1.4570. 1. R. and n.m.r. spectroscopy confirm the structure.

:EXAMPLE 1V 3 ,7-dimethyl-6-chlorol -p-ethylphenoxy-2,3-epoxy-7- octane VQTO' 1.17 gr. (0.004 mole) of the reaction product of Example 1 is dissolved in 10 ml. CH CI 0.004 mole of mchloroperbenzoic acid solution in CHgClg are slowly added dropwise at 0 to 5C. temperature: The mixture is stirred at room temperature overnight, then washed with 10 ml. NaHCO three times, dried over MgSO filtered and stripped to yield 0.9 grams of the desired product N 1.5160. The structure is confirmed by l.R., n.m.r. mass spectroscopy.

The following is a table of certain selected compounds that are preparable according to the procedures described hereto. Compound numbers are assigned to each compound and are used throughout the remainder of the specification.

TABLE 1 COMPOUND R1 R x A & B R

NUMBER 1 cu, cu, Cl bond 4CH,S- 2 CH CH, CH bond 4 c,i-| 3 CH1 CH3 Br bond 4-C,H5

TAB LE 1 Continued COMPOUND R R X A & B R

NUMBER 4 CH; CH; Cl bond H 5 CH; CH; Cl bond 4-CH; 6 CH; CH; Br bond 4iC;H, 7 CH; CH; Cl bond 4NO; 8 CH; CH; C] bond 3Cl 9 CH; CH; Br bond 4Cl 10 CH; CH; Cl bond 4-Br l 1 CH; CH; Cl bond 4-l l2 CH; CH; Br bond 4-F [3 CH; CH; Cl bond 4CN l4 CH; CH; Cl bond 3-CH;O- [5 CH; CH; Br bond 4CH;O [6 CH; CH; Cl bond 4C;H;O 17 CH; CH Br bond 4nC H;- 18 CH; CH; Br bond 4-CH;CH=CH 19 CH; CH; Cl bond 4CH;CH;CH(CH;) 20 CH; Ch; Br bond 4nC;H 21 CH; CH; Cl bond 3C;H; 22 CH; CH; Br bond 3C H; 23 CH; CH; Cl bond 4--sec.C;H; 24 CH; CH; Cl epoxide 4-C H; 25 1 CH; CH; Cl epoxide H 26 CH; CH; Br epoxide 4-CH; 27 CH; CH; Cl epoxide 4i--C;H 28 CH; CH; Cl epoxide 4NO; 29 CH; 'CH; Br epoxide 3-Cl 30 CH; CH; Cl epoxide 4-Cl 31 CH; CH; Cl epoxide 4-Br 32 CH; CH; Br epoxide 4-l 33 CH; CH; Cl epoxidc 4F 34 CH; CH; Cl epoxide 4-CN 35 CH; CH; Cl epoxide 3CH;O- 36 CH; CH; Br epoxide 4--CH;O 37 CH;' CH; Cl epoxide 4C,H -,O 38 CH; CH; Br epoxide 4nC;H; 39 CH; CH; Cl epoxide 4CH;S 40 CH; CH; Br epoxide 4CH;CH=CH 4| CH; CH; Cl epoxide 4CH;CH;CH(CH;) 42 CH; CH; Br epoxide 4-n-C;H; 43 CH; CH; Cl epoxide 3-C;H; 44 CH; CH; Br epoxide 3C;H; 45 CH; CH; Cl epoxidc 4sec.C;H; 46 CH; CH; Cl H H' 47 CH; CH; Cl H 4-CH; 48 CH; CH; Br H 4iC;H 49 CH; CH; Cl H 4NO; 50 CH; CH; Cl H 3-Cl 5! CH; CH; Br H 4--Cl 52 CH; CH; Cl H 4--Br 53 CH; CH; Cl H 4-] 54 CH; CH; Br H 4F 55 CH; CH; Cl H 4--CN 56 CH; CH; Cl H 3CH;O 57 CH; CH; Br H 4--CH;O 58 CH; CH; Cl H 4C;H;O 59 CH; CH; Br H 4-n--C H; 60 CH; CH; Cl H 4CH;S 61 CH; CH; Cl H 4-C;H; 62 CH; CH; Br H 4C;H; 6'! CH; CH; Br H 4CH;CH=CH 64 CH; CH; Cl H 4-CH;CH;CH(CH;) 65 CH; CH; Br H 4n-C;H; 66 CH; CH; Cl H 3C;H; 67 CH; CH; Br H 3C;H 68 CH; CH; Cl H 4sec.C.H;

INSECTICIDAL ESVALUATION TEST The degree of activity of a candidate compound to hinder or impede the metamorphosis of insects is measured by treating the penultimate larval stage of a representative insect with the compound and examining it after its last molt toward the adult form for retention of immature features.

Specifically, yellow mealworm, Tenebrio molitor, L., larvae are maintained at 28C. and 40% humidity on a diet of bran flakes. Prepupae care collected from the culture and kept in separate containers. The pupae collected once daily, are 1-25 hours old at the time of treatment. By means of a syringe, suitable amounts of candidate compounds in 0.5 or 1.0 ul of acetone are applied to the venter of Tenebrio nzolitor, L. pupae. Treated pupae are maintained at 28C. and 40% humidity until the adults emerged (usually within 6-8 days). Emerged adults are graded as positive. negative, or dead. To be considered a positive response. the presence of typical pupal cuticle, urogomphi, gin trap. and

TABLE 11 COMPOUND NUMBER EDsn'I Q/P Pa The compounds of this invention are generally embodied into a form suitable for convenient application. For example, the compounds can be embodied into pesticidal composition'which are provided in the form of emulsions, suspensions, solutions, dusts, and aerosol sprays. In general, such compositions will contain, in addition to the active compound, the adjuvants which are found normally in pesticide preparations. In these compositions, the active compounds of this invention can be employed as the sole pesticide component or they can be used in admixture with other compounds having similar. utility. The pesticide compositions of this invention can contain, as adjuvants, organic solvents, such as sesame oil, xylene range solvents, heavy petroleum, etc.; water; emulsifying agents; surface active agents; talc; pyrophyllite; diatomite; gypsum; clays, propelants, such as dichlorodifluoromethane, etc. If desired, however, the active compounds can be applied directly to feedstuffs, seeds, etc. upon which the pests feed. When applied in such a manner, it will be advantageous to use a compound which is not volatile. In connection with the activity of the presently disclosed pesticidal compounds, it should be fully understood that it is not necessary that they be active as such. The purposes of this invention will be fully served if the compound is rendered active by external influences, such as light or by some physiological action which occurs when the compound is ingested into the body of the pest.

The precise manner in which the pesticidal compositions of this invention are used in any particular instance will be readily apparent to a person skilled in the art. Generally, the active pesticide compound will be embodied in the form of a liquid composition, for example, an emulsion, suspension, or aerosol spray. While the concentration of the active pesticide in the present compositions can vary within rather wide limits, ordinarily the pesticide compound will comprise not more than about 15.0% by weight of the composition. Preferably, however, the pesticide compositions of this invention will be in the form of solutions or suspensions containing about 0.1 to 1.0% weight of the active pesticide compound.

What is claimed is:

l. A compound of the formula:

in which R is lower alkyl having 1 to 4 carbon atoms in the 3 or 4 position; X is chlorine or bromine; and A and B together form a bond.

2. The compound of claim 1 in which X is chlorine. 3. The compound of claim 1 in which X is bromine. 4. The compound of claim 3 in which R is 4-ethyl. 

1. A COMPOUND OF THE FORMULA:
 2. The compound of claim 1 in which X is chlorine.
 3. The compound of claim 1 in which X is bromine.
 4. The compound of claim 3 in which R is 4-ethyl. 